From ligand to complexes: inhibition of human immunodeficiency virus type 1 integrase by β-diketo acid metal complexes

Sechi, Mario, Bacchi, Alessia, Carcelli, Mauro, Compari, Carlotta, Duce, Elenia, Fisicaro, Emilia, Rogolino, Dominga, Gates, Paul, Derudas, Marco, Al-Mawsawi, Laith Q and Neamati, Nouri (2006) From ligand to complexes: inhibition of human immunodeficiency virus type 1 integrase by β-diketo acid metal complexes. Journal of Medicinal Chemistry, 49 (14). pp. 4248-4260. ISSN 0022-2623

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Abstract

β-Diketo acid-containing compounds are a promising class of human immunodeficiency virus type 1 (HIV-1) integrase (IN) inhibitors. Starting from the hypothesis that these inhibitors are able to coordinate ions in solution before interacting on the active site, a series of potentiometric measurements have been performed to understand the coordination ability of the diketo acid pharmacophore toward the biologically relevant Mg2+. Moreover, by using β-diketo acid/ester as model ligands with a set of divalent metal ions (Mg, Mn, Ni, Co, Cu, and Zn), we obtained a series of complexes and tested them for anti-HIV-1 IN activity. Results demonstrate that the diketo acid functionality chelates divalent metal ions in solution, and complexes with metals in different stoichiometric ratios are isolated. We postulate that the diketo acids act as complexes in their active form. In particular, they predominantly form species such as Mg2L2+ and Mg2L2 (derived from diketo acids, H2L), and MgL+ and MgL2 (derived from diketo esters, HL) at physiological pH. Furthermore, the synthesized mono- and dimetallic complexes inhibited IN at a high nanomolar to low micromolar range, with metal dependency in the phenyl diketo acid series. Retrospective analysis suggests that the electronic properties of the aromatic framework influence the metal-chelating ability of the diketo acid system. Therefore, the difference in activities is related to the complexes they preferentially form in solution, and these findings are important for the design of a new generation of IN inhibitors.

Item Type: Article
Schools and Departments: School of Life Sciences > Chemistry
Depositing User: Marco Derudas
Date Deposited: 28 Jul 2015 12:32
Last Modified: 28 Jul 2015 12:32
URI: http://srodev.sussex.ac.uk/id/eprint/55791
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